(Q42658082)

English

The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression

scientific article published on May 1997

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scholarly article

1 reference

Europe PubMed Central

4 November 2017

The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression (English)

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Europe PubMed Central

4 November 2017

neurodegeneration

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inferred from title

13

object named as

Lander ES

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Europe PubMed Central

4 November 2017

Mark Joseph Daly

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object named as

Daly MJ

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Europe PubMed Central

4 November 2017

author name string

Hamilton BA

1

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Europe PubMed Central

4 November 2017

Smith DJ

2

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Europe PubMed Central

4 November 2017

Mueller KL

3

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Europe PubMed Central

4 November 2017

Kerrebrock AW

4

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Europe PubMed Central

4 November 2017

Bronson RT

5

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Europe PubMed Central

4 November 2017

van Berkel V

6

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Europe PubMed Central

4 November 2017

Kruglyak L

8

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Europe PubMed Central

4 November 2017

Reeve MP

9

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Europe PubMed Central

4 November 2017

Nemhauser JL

10

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Europe PubMed Central

4 November 2017

Hawkins TL

11

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Europe PubMed Central

4 November 2017

Rubin EM

12

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Europe PubMed Central

4 November 2017

language of work or name

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publication date

1 May 1997

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Europe PubMed Central

4 November 2017

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Europe PubMed Central

4 November 2017

18

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4 November 2017

5

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Europe PubMed Central

4 November 2017

711-722

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Europe PubMed Central

4 November 2017

Aberrant transcription caused by the insertion of an early transposable element in an intron of the Fas antigen gene of lpr mice

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7 January 2021

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Basic local alignment search tool

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7 January 2021

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Characterization and expression of a cDNA specifying subunit VIIc of bovine cytochrome c oxidase

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7 January 2021

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The Saccharomyces cerevisiae SEC14 gene encodes a cytosolic factor that is required for transport of secretory proteins from the yeast Golgi complex

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7 January 2021

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An essential role for a phospholipid transfer protein in yeast Golgi function

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7 January 2021

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Isolation of a putative phospholipase C gene of Drosophila, norpA, and its role in phototransduction.

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

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The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinase

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7 January 2021

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Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration

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Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration

1 reference

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Frataxin fracas

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Phosphatidylinositol transfer protein dictates the rate of inositol trisphosphate production by promoting the synthesis of PIP2

1 reference

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7 January 2021

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Phosphoinositides as regulators in membrane traffic

1 reference

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7 January 2021

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Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells

1 reference

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A comprehensive genetic map of the mouse genome.

1 reference

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Role of type I myosins in receptor-mediated endocytosis in yeast

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Ciliary neurotrophic factor prevents neuronal degeneration and promotes low affinity NGF receptor expression in the adult rat CNS

1 reference

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7 January 2021

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Hereditary retinal degeneration in Drosophila melanogaster. A mutant defect associated with the phototransduction process

1 reference

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7 January 2021

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Mutant immunoglobulin genes have repetitive DNA elements inserted into their intervening sequences.

1 reference

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7 January 2021

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Resolution of regulated secretion into sequential MgATP-dependent and calcium-dependent stages mediated by distinct cytosolic proteins

1 reference

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7 January 2021

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Phosphatidylinositol transfer protein required for ATP-dependent priming of Ca(2+)-activated secretion

1 reference

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7 January 2021

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Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome

1 reference

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7 January 2021

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Requirement for phosphatidylinositol transfer protein in epidermal growth factor signaling

1 reference

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7 January 2021

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Construction of a large-insert yeast artificial chromosome library of the mouse genome

1 reference

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7 January 2021

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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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7 January 2021

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The Drosophila dgq gene encodes a G alpha protein that mediates phototransduction.

1 reference

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Ultrastructural observations on spinal ganglion biopsy in Friedreich's ataxia: a preliminary report

1 reference

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7 January 2021

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Signal transduction and membrane traffic: the PITP/phosphoinositide connection

1 reference

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7 January 2021

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Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway

1 reference

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7 January 2021

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Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene

1 reference

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7 January 2021

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A role for phosphatidylinositol transfer protein in secretory vesicle formation

1 reference

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Complementation of the beige mutation in cultured cells by episomally replicating murine yeast artificial chromosomes.

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Ciliary neurotrophic factor prevents the degeneration of motor neurons after axotomy.

1 reference

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7 January 2021

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Ciliary neurotrophic factor prevents degeneration of motor neurons in mouse mutant progressive motor neuronopathy

1 reference

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Photoreceptor deactivation and retinal degeneration mediated by a photoreceptor-specific protein kinase C.

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1 reference

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1 reference

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1 reference

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1 reference

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Identifiers

10.1016/S0896-6273(00)80312-8

1 reference

Europe PubMed Central

4 November 2017

1 reference

Europe PubMed Central

4 November 2017

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